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Structure of 885702-34-1
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4-Bromo-2-chloropyrimidine features a dual halogen substitution pattern that enables selective cross-coupling reactions in medicinal chemistry. The electron-deficient pyrimidine core facilitates nucleophilic aromatic substitution, while the bromo and chloro groups offer orthogonal reactivity for sequential functionalization. This compound serves as a key scaffold in kinase inhibitor development and other bioactive molecule architectures.
4-Bromo-2-chloropyrimidine serves as a versatile building block in medicinal chemistry, enabling selective cross-coupling and nucleophilic substitution reactions. Its complementary halogenation pattern facilitates sequential functionalization via Pd-catalyzed coupling or amination protocols. The molecule exhibits excellent bench stability and is compatible with a range of reaction conditions, making it ideal for constructing heterocyclic scaffolds and advanced intermediates in API development.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: